| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001205262.2 | 2826 | Intron | NP_001192191.1 | ||
| NM_001205263.1 | 2826 | Missense Mutation | ATT,GTT | I715V | NP_001192192.1 |
| NM_012415.3 | 2826 | Missense Mutation | ATT,GTT | I899V | NP_036547.1 |